Removal of per- and polyfluoroalkyl substances using super-fine powder activated carbon and ceramic membrane filtration

吸附 活性炭 化学 过滤(数学) 色谱法 水处理 污染 微滤 环境化学 化学工程 环境工程 环境科学 有机化学 统计 工程类 生态学 生物 生物化学 数学
作者
Conner C. Murray,Hooman Vatankhah,Carrie A. McDonough,Anastasia Nickerson,Tayler Hedtke,Tzahi Y. Cath,Christopher P. Higgins,Christopher Bellona
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:366: 160-168 被引量:106
标识
DOI:10.1016/j.jhazmat.2018.11.050
摘要

Contamination of drinking water sources with per- and polyfluoroalkyl substances (PFASs) is a major challenge for environmental engineers. While granular activated carbon (GAC) is an effective adsorbent-based treatment technology for long-chained PFASs, GAC is less effective for removal of short-chained compounds, necessitating a more complete treatment strategy. Super-fine powder activated carbon (SPAC; particle diameter <1 um) is potentially a superior adsorbent to GAC due to high specific surface area and faster adsorption kinetics. This study served to evaluate SPAC coupled with ceramic microfiltration (CMF) for PFAS removal in a continuous flow system. Comparison of PFAS mass loading rates onto SPAC and GAC to 10% breakthrough of PFASs using contaminated groundwater indicates that SPAC has nearly double the adsorption potential of GAC. Limitations reaching breakthrough for the SPAC system led to additional higher mass loading experiments where PFAS adsorption onto SPAC reached 2990 μg/g (for quantifiable PFASs), 480x greater than GAC and is thought to be a function of adsorbent size, pore content and PFAS chain length. Additional analysis of system performance through the application of liquid chromatography quadrupole time-of-flight mass spectrometry (LC-QToF-MS) revealed the presence of additional PFASs in influent samples that were removed by the SPAC/CMF system.

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